Canonical Allele Identifier: CA2091759533

Gene: THSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397628A= , CM000675.2:g.52397628A=	GRCh38
NC_000013.10:g.52971763A= , CM000675.1:g.52971763A=	GRCh37
NC_000013.9:g.51869764A=	NCBI36
NG_047168.1:g.13867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.625T= MANE Select	ENSP00000258613.4:p.Leu209=
ENST00000648254.1:c.625T=	ENSP00000497520.1:p.Leu209=
ENST00000258613.4:c.625T=	ENSP00000258613.4:p.Leu209=
ENST00000349258.8:c.625T=	ENSP00000340650.4:p.Leu209=
NM_018676.3:c.625T=	NP_061146.1:p.Leu209=
NM_199263.2:c.625T=	NP_954872.1:p.Leu209=
NM_018676.4:c.625T= MANE Select	NP_061146.1:p.Leu209=
NM_199263.3:c.625T=	NP_954872.1:p.Leu209=